Canonical Allele Identifier: CA359726207
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs2111723683

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233490G>A , CM000667.2:g.55233490G>A GRCh38
NC_000005.9:g.54529318G>A , CM000667.1:g.54529318G>A GRCh37
NC_000005.8:g.54565075G>A NCBI36
NG_034201.1:g.5228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.34C>T MANE Select ENSP00000282572.4:p.Pro12Ser
ENST00000282572.4:c.34C>T ENSP00000282572.4:p.Pro12Ser
ENST00000501463.2:c.34C>T ENSP00000422485.1:p.Pro12Ser
NM_021147.4:c.34C>T NP_066970.3:p.Pro12Ser
NR_125346.1:n.228C>T
NR_125347.1:n.228C>T
NM_021147.5:c.34C>T MANE Select NP_066970.3:p.Pro12Ser
NR_125346.2:n.119C>T
NR_125347.2:n.119C>T